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An Intervention to Reduce Prehospital Delay to Treatment in Acute Coronary Syndrome

Reducing Prehospital Delay in Acute Myocardial Infarction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00734760
Acronym
PROMOTION
Enrollment
3522
Registered
2008-08-14
Start date
2001-02-28
Completion date
2006-06-30
Last updated
2008-08-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndrome

Keywords

patient education, acute coronary syndrome, prehospital delay to treatment

Brief summary

This study was conducted to test whether a focused education and counseling intervention delivered by a nurse will decrease time of delay in seeking treatment for the signs and symptoms of acute coronary syndrome (i.e., heart attack) in patients already identified as having ischemic heart disease.

Detailed description

Delay to treatment from the onset acute coronary syndrome (ACS)continues to be a significant cause of morbidity and mortality. This study was conducted to evaluate a tailored education and counseling program designed for individuals at high risk for a future event. Study Hypothesis: The central hypothesis of this study was that a focused education and counseling intervention delivered by a nurse will decrease time of delay in seeking treatment for the signs and symptoms of AMI in patients already identified as having ischemic heart disease. Patients were randomized to receive a nurse-administered education and counseling intervention designed to promote early presentation for medical treatment in the face of cardiac symptoms or to usual instructions by their healthcare provider. Primary & Secondary Endpoints: The primary endpoint of this trial was prehospital delay time, i.e., time from onset of symptoms to arrival at the hospital. The secondary endpoints were: use of the emergency medical system; use of aspirin; healthcare resource utilization; and knowledge, attitudes and beliefs about heart disease.

Interventions

BEHAVIORALeducation

face-to-face education and counseling intervention

Sponsors

University of California, San Francisco
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* a diagnosis of ischemic heart disease, confirmed by their physician or medical record * lived independently (i.e., not in an institutional setting).

Exclusion criteria

* complicating serious co-morbidity such as a psychiatric illness or untreated malignancy * neurological disorder with impaired cognition * inability to read or understand English. * major uncorrected hearing loss

Design outcomes

Primary

MeasureTime frame
time from ACS symptom onset to admission to emergency departmenttwo years

Secondary

MeasureTime frame
pre-hospital aspirin usetwo years
emergency medical system usetwo years
resource utilizationtwo years

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026